Hyperproinsulinemia
human disease
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Hyperproinsulinemia
Summary
Hyperproinsulinemia is a rare disease[1].
Key Facts
- Hyperproinsulinemia's instance of is recorded as rare disease[2].
- Hyperproinsulinemia's instance of is recorded as disease[3].
- Hyperproinsulinemia's subclass of is recorded as genetic disease[4].
- Hyperproinsulinemia's subclass of is recorded as diabetes[5].
- Hyperproinsulinemia's MeSH descriptor ID is recorded as C562776[6].
- Hyperproinsulinemia's OMIM ID is recorded as 616214[7].
- Hyperproinsulinemia's ICD-9-CM is recorded as 250.80[8].
- Hyperproinsulinemia's genetic association is recorded as INS[9].
- Hyperproinsulinemia's UMLS CUI is recorded as C0342283[10].
- Hyperproinsulinemia's Mondo ID is recorded as MONDO_0014535[11].
- Hyperproinsulinemia's Microsoft Academic ID is recorded as 2779670698[12].
- Hyperproinsulinemia's UniProt disease ID is recorded as DI-01585[13].
- Hyperproinsulinemia's Experimental Factor Ontology ID is recorded as 0009650[14].